Canonical Allele Identifier: PA2825942901
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 30045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asn1954Lys
CA019555
NM_001160160.2:c.5862C>A
CA352139301
NM_001160160.2:c.5862C>G